HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643261Generated: October 27, 2026
Piperidine → 2-Piperidin-1-yl-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide
https://huagongshe.com/reaction/643261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-chloro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide | HCID 68429657 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Piperidin-1-yl-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide | HCID 11234911 | 95.8% |
Reaction Steps
A solution of 2-chloro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide (40 mg, 0.115 mmol) in acetone (250 μl) was added to a mixture of piperidine (17.1 μl, 0.173 mmol) and DIPEA (40 μl, 0.229 mmol) in MeCN (250 μl). The resulting reaction mixture was heated and stirred in a microwave oven for 10 min. at 100° C. After cooling to room temperature the volatiles were removed in vacuo and the residue purified on a prep. Gilson HPLC. Pure fractions were collected, evaporated in vauco and dried at 50° C. for 16 hours affording 43.8 mg (75%) of the title compounds as a TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700583B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-b521292d31e14319a593a534ebda5712 |
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| Source note | uspto-grants-2010_04 |
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